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NCT ID: NCT05817890 Active, not recruiting - Healthy Clinical Trials

Absorption, Metabolism, and Excretion of CYC065 in Healthy Male Subjects

Start date: March 3, 2023
Phase: Early Phase 1
Study type: Interventional

This will be a Phase 1, open-label, single dose study of the Absorption, Metabolism, and Excretion of CYC065 in healthy male subjects.

NCT ID: NCT05817643 Active, not recruiting - Alzheimer Disease Clinical Trials

Food Effect Study of BMS-984923 in Healthy Older Adult Volunteers

Start date: January 10, 2023
Phase: Phase 1
Study type: Interventional

This project is developing a novel disease-modifying compound for Alzheimer's disease (AD).

NCT ID: NCT05817383 Active, not recruiting - Depressive Symptoms Clinical Trials

Berries, Bugs, and the Blues

Start date: April 5, 2023
Phase: N/A
Study type: Interventional

This study aims to investigate the impact of daily freeze-dried blueberry powder consumption on the gut microbiota, fecal short chain fatty acids, and depressive symptom severity in 40older, sedentary adults with depressive symptoms.

NCT ID: NCT05816564 Active, not recruiting - Depression Clinical Trials

Optimizing Attentional Bias Modification

Start date: October 1, 2022
Phase: N/A
Study type: Interventional

Depression has been associated with an attention bias towards negative information. Attention bias modification (ABM) interventions explore potential benefits of training attention away from negative or threatening information and towards neutral or positive information. The goal of this study is to examine the effectiveness of an ABM intervention that includes a preceding mindfulness training among a sample of individuals who self-reported mild-to-moderately depression symptoms. The main question this study aims to answer is: • Do individuals who participate in an ABM intervention have a greater reduction in attention bias towards negative information and depressive symptoms when compared to a control group? Participants will be asked to participate in 3 days of brief mindfulness training exercises preceding an ABM intervention session that lasts 1.5 to 2 hours while wearing electroencephalography (EEG) equipment. Researchers will compare the ABM intervention group to a "sham" intervention group to see if the ABM intervention reduces negative attention bias above and beyond brief mindfulness training.

NCT ID: NCT05816551 Active, not recruiting - Aging Clinical Trials

Aging and Gastrointestinal Barrier Function

Start date: July 1, 2023
Phase:
Study type: Observational

The purpose of this study is to assess the gastrointestinal responses of the elderly during hyperthermia.

NCT ID: NCT05816395 Active, not recruiting - Clinical trials for Osteoarthritis, Knee

Safety and Efficacy of RHH646 for Knee Osteoarthritis

Start date: May 31, 2023
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the articular cartilage-regenerating capacity of RHH646 in the knee as well as to assess safety and tolerability in participants with knee osteoarthritis. The treatment duration will be up to 52 weeks. The total study duration for an individual participant will be up to 62 weeks.

NCT ID: NCT05815498 Active, not recruiting - COVID-19 Clinical Trials

A Study of mRNA-1283.222 Injection Compared With mRNA-1273.222 Injection in Participants ≥12 Years of Age to Prevent COVID-19

NextCOVE
Start date: March 28, 2023
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety, reactogenicity, and relative vaccine efficacy (rVE) of the mRNA-1283.222 vaccine as well as its immunogenicity in comparison to the mRNA-1273.222 vaccine.

NCT ID: NCT05814757 Active, not recruiting - Dry Eye Syndromes Clinical Trials

OTX-DED for the Short-term Treatment of the Symptoms of Dry Eye Disease (DED)

Start date: May 11, 2023
Phase: Phase 2
Study type: Interventional

To assess the efficacy and safety of OTX-DED for the short-term treatment of the symptoms of DED

NCT ID: NCT05814562 Active, not recruiting - Hypertension Clinical Trials

Cardiovascular Precision Medicine & Remote Intervention

CP&R
Start date: April 10, 2023
Phase: N/A
Study type: Interventional

This exploratory / proof of concept study aims to evaluate whether it is possible to identify at-risk patients based on EHR review of blood pressure fluctuation over time and cholesterol levels, recruit those patients, and engage them in a remote intervention protocol.

NCT ID: NCT05814419 Active, not recruiting - Clinical trials for Familial Hyperlipidemia

Familial Hyperlipidemia Family Registry

Start date: February 17, 2023
Phase:
Study type: Observational [Patient Registry]

The aim of the study is to identify children and families that are at risk for cardiovascular disease because of a condition known as familial hyperlipidemia. This condition may increase the risk of cardiac events such as hardening of the arteries anywhere in the body which can result in heart attacks, strokes, and death over ten fold. Children have already been assessed in the Healthy Hearts screening program and identified as having elevated cholesterol. A buccal smear will identify whether the familial hyperlipidemia condition exist in your child. If the child's test shows that they have the specific gene for familial hyperlipidemia and shows a genetic tendency towards premature heart disease, we would encourage genetic testing for as many blood family members as possible. The study plan is to determine whether the Healthy Hearts screening program is a more effective way of identifying students at risk since it is estimated that less than 10% of those individuals with the problem have been identified. If it is effective, then it will be incorporated as part of the standard screening process in the Healthy Hearts program. Aim 1: Is a school screening program a more effective method to identifying those at risk for familial hyperlipidemia? Aim 2: What percent of children with elevated cholesterol ≥ 200 mg/dl have familial hyperlipidemia?